Canonical Allele Identifier: PA162772
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 135440
ClinVar RCV Id: RCV000122297 RCV000234534 RCV001550970 RCV003315786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Val1339Ile
CA162770
NM_000553.6:c.4015G>A