Allele Registry

Canonical Allele Identifier: PA214561

Gene: MCM8 HGNC NCBI

ClinVar Allele:

171038

ClinVar RCV:

RCV000148343

RCV000162356

ClinVar Variation:

161191

HGVS (amino-acid)	Matching Registered Transcripts
NP_115874.3:p.Pro149Arg	CA214559 NM_032485.6:c.446C>G