Allele Registry

Canonical Allele Identifier: PA658664975

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000540807

RCV000633192

RCV004025425

ClinVar Variation:

458501

528108

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg279Trp	CA4704170 NM_000553.6:c.835C>T CA658657759 NM_000553.6:c.834_835delinsTT