Canonical Allele Identifier: PA2826444740
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Gly165Arg
CA411096875
NM_001257387.2:c.493G>C
CA411096877
NM_001257387.2:c.493G>A