Canonical Allele Identifier: PA2827474064
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2183472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser28Tyr
CA411091620
NM_001349956.2:c.83C>A