Canonical Allele Identifier: PA2827476794
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786420
ClinVar RCV Id: RCV002417797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Glu293Asp
CA411097510
NM_001349956.2:c.879G>T
CA411097517
NM_001349956.2:c.879G>C