Canonical Allele Identifier: PA2825276519
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 924789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Gln29Pro
CA411091598
NM_001005735.2:c.86A>C