Canonical Allele Identifier: PA2825276682
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 481099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Asp77Val
CA411090674
NM_001005735.2:c.230A>T