Canonical Allele Identifier: PA2573170463
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1387333
ClinVar RCV Id: RCV001883996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Cys1041Arg
CA370922546
NM_000553.6:c.3121T>C