Canonical Allele Identifier: PA2830301967
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ala363Val
CA164560
NM_145862.2:c.1088C>T