Allele Registry

Canonical Allele Identifier: PA2499233515

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV001314876

ClinVar Variation:

1015945

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg369Gly	CA370920739 NM_000553.6:c.1105C>G