Allele Registry

Canonical Allele Identifier: PA645437348

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000229443

RCV001357192

ClinVar Variation:

238143

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ile912Ser	CA4704842 NM_000553.6:c.2735T>G