Canonical Allele Identifier: PA915954318
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Pro436Leu
CA299082
NM_001005735.2:c.1307C>T