Canonical Allele Identifier: PA2825861911
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2193352
ClinVar RCV Id: RCV002623939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Ser125Pro
CA397859203
NM_001143992.2:c.373T>C