Canonical Allele Identifier: PA2825861216
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663449
ClinVar RCV Id: RCV003442637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Ser54Tyr
CA397856804
NM_001143990.2:c.161C>A