Canonical Allele Identifier: PA2829689775
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 848666
ClinVar RCV Id: RCV001052474 RCV001271232 RCV003455230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Pro1076Ser
CA1396048
NM_007123.6:c.3226C>T