Canonical Allele Identifier: PA2580122231
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1982784
ClinVar RCV Id: RCV002766884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Thr1417Ser
CA370911750
NM_000553.6:c.4249A>T
CA370911758
NM_000553.6:c.4250C>G