Canonical Allele Identifier: PA2829689511
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2537569
ClinVar RCV Id: RCV003256102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg930Trp
CA344864037
NM_007123.6:c.2788A>T