Canonical Allele Identifier: PA2829700269
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Gly386Arg
CA411096875
NM_007194.4:c.1156G>C
CA411096877
NM_007194.4:c.1156G>A