Canonical Allele Identifier: PA164059
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Val25Ile
CA164058
NM_007194.4:c.73G>A