Canonical Allele Identifier: PA658665206
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 458480
ClinVar RCV Id: RCV000525485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Phe1411Leu
CA370911665
NM_000553.6:c.4231T>C
CA370911676
NM_000553.6:c.4233T>A
CA370911677
NM_000553.6:c.4233T>G