Canonical Allele Identifier: PA2830303464
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Thr504Ala
CA167185
NM_145862.2:c.1510A>G