Canonical Allele Identifier: PA2825861569
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502371
ClinVar RCV Id: RCV002020205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137463.1:p.Leu113Pro
CA287495002
NM_001143991.2:c.338T>C