Canonical Allele Identifier: PA645498798
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Val314Leu
CA16616586
NM_007194.4:c.940G>T
CA411099989
NM_007194.4:c.940G>C