Canonical Allele Identifier: PA2829689430
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2097074
ClinVar RCV Id: RCV003016505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asn880Tyr
CA344864370
NM_007123.6:c.2638A>T