Allele Registry

Canonical Allele Identifier: PA162787

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122302

RCV000464655

RCV000543218

RCV001753506

ClinVar Variation:

135445

458487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Thr172Pro	CA162785 NM_000553.6:c.514A>C CA658657758 NM_000553.6:c.513_514delinsTC