Canonical Allele Identifier: PA2829690489
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 295423
ClinVar RCV Id: RCV000280684 RCV000335820 RCV001470224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg1471Thr
CA1395711
NM_007123.6:c.4412G>C