Canonical Allele Identifier: PA2830301915
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Gly357Arg
CA411096875
NM_145862.2:c.1069G>C
CA411096877
NM_145862.2:c.1069G>A