Canonical Allele Identifier: PA916077092
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser49Cys
CA299099
NM_145862.2:c.146C>G