Canonical Allele Identifier: PA2829689799
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524532
ClinVar RCV Id: RCV002031790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asp1101Tyr
CA344862338
NM_007123.6:c.3301G>T