Canonical Allele Identifier: PA2829688168
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 438026
ClinVar RCV Id: RCV000504853 RCV001360100 RCV002470889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg274Gly
CA1396686
NM_007123.6:c.820C>G