Canonical Allele Identifier: PA2829689762
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1390129
ClinVar RCV Id: RCV001917521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gln1063His
CA344862582
NM_007123.6:c.3189A>T
CA344862583
NM_007123.6:c.3189A>C