Canonical Allele Identifier: PA253492
Gene: WRN HGNC NCBI
ClinVar RCV:
RCV000005783
ClinVar Variation:
5450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Gln1229Leu
CA253490
NM_000553.6:c.3686A>T