Canonical Allele Identifier: PA156025
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 130760
ClinVar RCV Id: RCV000118878 RCV000312662 RCV001668268 RCV003315693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Val114Ile
CA156023
NM_000553.6:c.340G>A