Canonical Allele Identifier: PA2830302177
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 926661
ClinVar RCV Id: RCV001189357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ile387Ser
CA411096555
NM_145862.2:c.1160T>G