Allele Registry

Canonical Allele Identifier: PA645437384

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000468223

RCV003972753

ClinVar Variation:

404055

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Arg1020His	CA4704927 NM_000553.6:c.3059G>A