Allele Registry

Canonical Allele Identifier: PA2826588862

Gene: MCM8 HGNC NCBI

ClinVar RCV:

RCV000148343

RCV000162356

ClinVar Variation:

161191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268451.1:p.Pro149Arg	CA214559 NM_001281522.2:c.446C>G