Canonical Allele Identifier: PA2825276536
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 818300
ClinVar RCV Id: RCV001009772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser35Pro
CA411091469
NM_001005735.2:c.103T>C