Canonical Allele Identifier: PA2825276659
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Gln69His
CA10168060
NM_001005735.2:c.207G>C
CA411090788
NM_001005735.2:c.207G>T