Allele Registry

Canonical Allele Identifier: PA162769

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122296

RCV000547973

ClinVar Variation:

135439

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Pro1376Leu	CA162767 NM_000553.6:c.4127C>T