Canonical Allele Identifier: PA2829689468
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1976221
ClinVar RCV Id: RCV002760781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Leu908Ser
CA344864172
NM_007123.6:c.2723T>C