Canonical Allele Identifier: PA162739
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 135429
ClinVar RCV Id: RCV000122286 RCV000230775 RCV000726887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Asp996Asn
CA162737
NM_000553.6:c.2986G>A