Allele Registry

Canonical Allele Identifier: PA271062

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000145146

RCV000891999

ClinVar Variation:

157835

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Gly1837Asp	CA271061 NM_018136.5:c.5510G>A