Allele Registry

Canonical Allele Identifier: PA162706

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122275

RCV000552831

ClinVar Variation:

135419

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser612Cys	CA162704 NM_000553.6:c.1835C>G