Canonical Allele Identifier: PA2829689180
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1503259
ClinVar RCV Id: RCV002045391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Leu736Phe
CA1396265
NM_007123.6:c.2206C>T