Canonical Allele Identifier: PA2827474047
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 949613
ClinVar RCV Id: RCV001221109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gln27His
CA411091632
NM_001349956.2:c.81G>T
CA411091634
NM_001349956.2:c.81G>C