Canonical Allele Identifier: PA2829689977
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000767
ClinVar RCV Id: RCV001296940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Cys1195Arg
CA344868123
NM_007123.6:c.3583T>C