Canonical Allele Identifier: PA2829689201
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 546288
ClinVar RCV Id: RCV000658141 RCV001074375 RCV001199791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Cys744Tyr
CA1396259
NM_007123.6:c.2231G>A