Canonical Allele Identifier: PA2825861868
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663449
ClinVar RCV Id: RCV003442637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Ser54Tyr
CA397856804
NM_001143992.2:c.161C>A