Allele Registry

Canonical Allele Identifier: PA2826287299

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV003343172

ClinVar Variation:

2604049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Arg500Ser	CA344015918 NM_001206846.2:c.1500G>T CA344015921 NM_001206846.2:c.1500G>C