Canonical Allele Identifier: PA196769
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ala190Val
CA196768
NM_007194.4:c.569C>T