Canonical Allele Identifier: PA2827476706
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Glu284Asp
CA167545
NM_001349956.2:c.852G>T
CA411097656
NM_001349956.2:c.852G>C