Allele Registry

Canonical Allele Identifier: PA166628

Gene: CHEK2 HGNC NCBI

ClinVar RCV:

RCV000130543

RCV000197078

RCV000587712

RCV000764367

ClinVar Variation:

141856

HGVS (amino-acid)	Matching Registered Transcripts
NP_009125.1:p.Leu512Val	CA166627 NM_007194.4:c.1534C>G