Canonical Allele Identifier: PA167546
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Glu351Asp
CA167545
NM_007194.4:c.1053G>T
CA411097656
NM_007194.4:c.1053G>C