Allele Registry

Canonical Allele Identifier: PA156022

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000118877

RCV000281792

RCV000835593

RCV001434072

RCV003315692

ClinVar Variation:

130759

728015

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Leu1074Phe	CA156020 NM_000553.6:c.3222G>T CA370923188 NM_000553.6:c.3222G>C