Allele Registry

Canonical Allele Identifier: PA1139737297

Gene: ASPM HGNC NCBI

ClinVar Variation Id: 876853

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Ile1662Ser	CA1309830 NM_018136.5:c.4985T>G