Allele Registry

Canonical Allele Identifier: PA645437388

Gene: WRN HGNC NCBI

ClinVar Variation Id: 238146

HGVS (amino-acid)	Matching Registered Transcripts
NP_000544.2:p.Tyr1034Phe	CA4704933 NM_000553.6:c.3101A>T