Canonical Allele Identifier: PA2825861206
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2783651
ClinVar RCV Id: RCV003666186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Asp37Ala
CA397856000
NM_001143990.2:c.110A>C