Allele Registry

Canonical Allele Identifier: PA162763

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122294

RCV000228973

RCV000727484

ClinVar Variation:

135437

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Ser1292Tyr	CA162761 NM_000553.6:c.3875C>A