Canonical Allele Identifier: PA2829689488
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1311679
ClinVar RCV Id: RCV001752662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gly918Val
CA344864108
NM_007123.6:c.2753G>T