Canonical Allele Identifier: PA2829689834
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2156339
ClinVar RCV Id: RCV003075412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Leu1115Arg
CA37505095
NM_007123.6:c.3344T>G