Canonical Allele Identifier: PA2830302083
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Arg377Cys
CA294433
NM_145862.2:c.1129C>T