Allele Registry

Canonical Allele Identifier: PA202014

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000145242

RCV000176582

RCV000991554

RCV003905254

ClinVar Variation:

157919

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Arg3304Gln	CA202013 NM_018136.5:c.9911G>A