Canonical Allele Identifier: PA2826444712
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 818397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Thr157Ser
CA411096985
NM_001257387.2:c.470C>G
CA411097001
NM_001257387.2:c.469A>T