Canonical Allele Identifier: PA658665052
Gene: WRN HGNC NCBI
ClinVar RCV:
RCV000551629
ClinVar Variation:
458406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Ser707Gly
CA4704651
NM_000553.6:c.2119A>G