Canonical Allele Identifier: PA2829689187
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 623725
ClinVar RCV Id: RCV000761706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asn740Tyr
CA344865560
NM_007123.6:c.2218A>T