Allele Registry

Canonical Allele Identifier: PA645437436

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000462991

RCV003153572

ClinVar Variation:

404001

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Gly1298Val	CA4705201 NM_000553.6:c.3893G>T