Canonical Allele Identifier: PA916077186
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 582573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Trp93Ser
CA411090405
NM_145862.2:c.278G>C