Allele Registry

Canonical Allele Identifier: PA162748

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122289

RCV000733018

RCV001085837

RCV003315785

RCV003925216

ClinVar Variation:

135432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg36Gln	CA162746 NM_000553.6:c.107G>A