Allele Registry

Canonical Allele Identifier: PA162745

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122288

RCV000724001

RCV001083827

RCV003915221

ClinVar Variation:

135431

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser1141Leu	CA162743 NM_000553.6:c.3422C>T