Canonical Allele Identifier: PA658665208
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 458481
ClinVar RCV Id: RCV000540193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Lys1419Thr
CA4705308
NM_000553.6:c.4256A>C