Allele Registry

Canonical Allele Identifier: PA162796

Gene: WRN HGNC NCBI

ClinVar RCV:

RCV000122305

RCV000533817

RCV003935170

ClinVar Variation:

135448

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Asn240Lys	CA162794 NM_000553.6:c.720T>G CA370917195 NM_000553.6:c.720T>A