Allele Registry

Canonical Allele Identifier: PA2826287783

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000383545

RCV002059413

RCV002519459

ClinVar Variation:

294595

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Gly1781Arg	CA1308795 NM_001206846.2:c.5341G>A CA343997849 NM_001206846.2:c.5341G>C