Allele Registry

Canonical Allele Identifier: PA162733

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122284

RCV000456321

RCV001579799

RCV003153404

ClinVar Variation:

135427

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg993His	CA162731 NM_000553.6:c.2978G>A