Canonical Allele Identifier: PA2830302839
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Pro455Leu
CA294010
NM_145862.2:c.1364C>T