Canonical Allele Identifier: PA2827477042
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gly319Arg
CA411096875
NM_001349956.2:c.955G>C
CA411096877
NM_001349956.2:c.955G>A