Canonical Allele Identifier: PA2829689298
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1029379
ClinVar RCV Id: RCV001330637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Pro804Ser
CA344864858
NM_007123.6:c.2410C>T