Canonical Allele Identifier: PA658800108
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 528099
ClinVar RCV Id: RCV000633182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Leu6Met
CA4703957
NM_000553.6:c.16T>A