Canonical Allele Identifier: PA2573170638
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1478926
ClinVar RCV Id: RCV001990818
ClinVar Variation Id: 1524013
ClinVar RCV Id: RCV002049040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Gly1414Arg
CA4705303
NM_000553.6:c.4240G>C
CA370911708
NM_000553.6:c.4240G>A