Canonical Allele Identifier: PA2826444774
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Pro172Leu
CA299082
NM_001257387.2:c.515C>T