Canonical Allele Identifier: PA2829690170
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 498303
ClinVar RCV Id: RCV000597228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Val1296Ala
CA1395880
NM_007123.6:c.3887T>C