Canonical Allele Identifier: PA2829689765
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 557605
ClinVar RCV Id: RCV000673768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ser1068del
CA528749018
NM_007123.6:c.3202_3204del