Canonical Allele Identifier: PA2829689289
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1517234
ClinVar RCV Id: RCV002041035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asp798Asn
CA344864892
NM_007123.6:c.2392G>A