Canonical Allele Identifier: PA2573171212
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1437868
ClinVar RCV Id: RCV001957699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Tyr212Cys
CA4704114
NM_000553.6:c.635A>G