Canonical Allele Identifier: PA915954688
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Pro527Thr
CA299090
NM_001005735.2:c.1579C>A