Canonical Allele Identifier: PA2825277147
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Glu345Asp
CA288327
NM_001005735.2:c.1035A>C
CA411100896
NM_001005735.2:c.1035A>T