Canonical Allele Identifier: PA168193
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Lys317Glu
CA168192
NM_007194.4:c.949A>G