Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.6629A>T
p.Gln2210Leu (Legacy AA No. 2182)
Variant Type:
Point
Domain:
d5C2
Location:
Exon 25
Variant Effect:
Missense
Codon Change:
6629A>T
No. of Patients Reported:
1
Phenotype:
NA
Association:
Unknown
Allele Count *:
NA
Allele Number *:
NA
Allele Frequency *:
NA
References and Comments:
NCBI Clinvar Variation ID: 293571NA