Canonical Allele Identifier: PA2825276706
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 662401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Glu86Asp
CA411090539
NM_001005735.2:c.258G>T
CA411090540
NM_001005735.2:c.258G>C