Canonical Allele Identifier: PA891849711
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571406
ClinVar RCV Id: RCV000692543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Thr65Ala
CA411090825
NM_007194.4:c.193A>G