Canonical Allele Identifier: PA658664904
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 458425
ClinVar RCV Id: RCV000547889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Thr9Ala
CA4703958
NM_000553.6:c.25A>G