Allele Registry

Canonical Allele Identifier: PA299117

Gene: CHEK2 HGNC NCBI

ClinVar RCV:

RCV000160455

ClinVar Variation:

182455

HGVS (amino-acid)	Matching Registered Transcripts
NP_009125.1:p.Arg181Gly	CA299116 NM_007194.4:c.541C>G