Canonical Allele Identifier: PA2829689294
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 957934
ClinVar RCV Id: RCV001231005 RCV001834000 RCV003887929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ala800Thr
CA37501376
NM_007123.6:c.2398G>A