Canonical Allele Identifier: PA299091
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Pro484Thr
CA299090
NM_007194.4:c.1450C>A