Canonical Allele Identifier: PA2829689476
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48490
ClinVar RCV Id: RCV000041816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Thr911Asn
CA143446
NM_007123.6:c.2732C>A