Canonical Allele Identifier: PA2741820731
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2632224
ClinVar RCV Id: RCV003406066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Lys1420Arg
CA370911801
NM_000553.6:c.4259A>G