Canonical Allele Identifier: PA1139745884
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 970938
ClinVar RCV Id: RCV001246601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Gly37Ser
CA411091426
NM_145862.2:c.109G>A