Canonical Allele Identifier: PA645437466
Gene: WRN HGNC NCBI
ClinVar RCV:
RCV000332436
ClinVar Variation:
362816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Ile1394Val
CA4705275
NM_000553.6:c.4180A>G