Canonical Allele Identifier: PA2573171198
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1483341
ClinVar RCV Id: RCV002025417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Lys182Arg
CA370915989
NM_000553.6:c.545A>G