Canonical Allele Identifier: PA2499233616
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1051020
ClinVar RCV Id: RCV001359001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Tyr218Phe
CA370916444
NM_000553.6:c.653A>T