Canonical Allele Identifier: PA156022
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 130759
ClinVar RCV Id: RCV000118877 RCV000281792 RCV000835593 RCV003315692
ClinVar Variation Id: 728015
ClinVar RCV Id: RCV001434072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Leu1074Phe
CA156020
NM_000553.6:c.3222G>T
CA370923188
NM_000553.6:c.3222G>C