Canonical Allele Identifier: PA2825276618
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 570586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Gly58Ala
CA411090903
NM_001005735.2:c.173G>C