Canonical Allele Identifier: PA2825277169
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 530077
ClinVar Variation Id: 2701274
ClinVar RCV Id: RCV003501097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Gly350Arg
CA411100143
NM_001005735.2:c.1048G>C
CA411100147
NM_001005735.2:c.1048G>A