Canonical Allele Identifier: PA2580119955
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1916791
ClinVar RCV Id: RCV002625422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Phe203Leu
CA370916256
NM_000553.6:c.607T>C
CA370916261
NM_000553.6:c.609T>A
CA370916263
NM_000553.6:c.609T>G