Canonical Allele Identifier: PA2829690600
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3028726
ClinVar RCV Id: RCV003890591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Tyr1527Cys
CA344863599
NM_007123.6:c.4580A>G