Canonical Allele Identifier: PA2741818816
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2743174
ClinVar RCV Id: RCV003504586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Trp200Leu
CA370916227
NM_000553.6:c.599G>T