Canonical Allele Identifier: PA2829689421
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1403863
ClinVar RCV Id: RCV001901347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gly876Arg
CA344864392
NM_007123.6:c.2626G>C