Canonical Allele Identifier: PA1139669455
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 942304
ClinVar RCV Id: RCV001212265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Leu211Val
CA174844832
NM_000553.6:c.631C>G