Canonical Allele Identifier: PA2827474011
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Val25Ala
CA288324
NM_001349956.2:c.74T>C