Canonical Allele Identifier: PA645437474
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 403982
ClinVar RCV Id: RCV000475184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Arg1427Thr
CA4705313
NM_000553.6:c.4280G>C