Canonical Allele Identifier: PA658665188
Gene: WRN HGNC NCBI
ClinVar RCV:
RCV000546368
ClinVar Variation:
458471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Ala1294Val
CA4705198
NM_000553.6:c.3881C>T