Canonical Allele Identifier: PA2829689377
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 966629
ClinVar RCV Id: RCV001241356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asp850His
CA344864558
NM_007123.6:c.2548G>C