Canonical Allele Identifier: PA916077229
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410013
ClinVar RCV Id: RCV000459397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Leu106Val
CA16616348
NM_145862.2:c.316C>G