Allele Registry

Canonical Allele Identifier: PA162724

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122281

RCV000233425

RCV003315783

ClinVar Variation:

135424

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ile979Met	CA162722 NM_000553.6:c.2937T>G