Canonical Allele Identifier: PA2825861912
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2009169
ClinVar RCV Id: RCV002838145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Glu130Lys
CA397859485
NM_001143992.2:c.388G>A