Canonical Allele Identifier: PA2829690212
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2202968
ClinVar RCV Id: RCV002634345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Pro1320Leu
CA344867102
NM_007123.6:c.3959C>T