Canonical Allele Identifier: PA2829689482
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1396332
ClinVar RCV Id: RCV001902956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ile916Val
CA1396178
NM_007123.6:c.2746A>G