Allele Registry

Canonical Allele Identifier: PA162805

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122308

RCV000470767

RCV002469016

ClinVar Variation:

135451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser323Leu	CA162803 NM_000553.6:c.968C>T