Canonical Allele Identifier: PA2829689414
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 550022
ClinVar RCV Id: RCV000664639 RCV001868195 RCV003451626 RCV003451625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gly873Arg
CA37501180
NM_007123.6:c.2617G>A
CA344864410
NM_007123.6:c.2617G>C