Allele Registry

Canonical Allele Identifier: PA2825861220

Gene: WRAP53 HGNC NCBI

ClinVar Allele:

256465

ClinVar RCV:

RCV000253368

RCV000354405

RCV000989732

RCV001516489

RCV002418084

ClinVar Variation:

261001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001137462.1:p.Arg68Gly	CA8354906 NM_001143990.2:c.202C>G