Allele Registry

Canonical Allele Identifier: PA645437036

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000456237

RCV003153573

ClinVar Variation:

404029

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Thr461Met	CA4704342 NM_000553.6:c.1382C>T