Allele Registry

Canonical Allele Identifier: PA162697

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122272

RCV000226111

RCV003237732

ClinVar Variation:

135416

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Glu510Asp	CA162695 NM_000553.6:c.1530A>T CA370924648 NM_000553.6:c.1530A>C