Canonical Allele Identifier: PA2825276938
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ile294Phe
CA288326
NM_001005735.2:c.880A>T