Allele Registry

Canonical Allele Identifier: PA2826287339

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000194627

RCV000314198

RCV002517052

ClinVar Variation:

210348

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Val614Leu	CA208920 NM_001206846.2:c.1840G>C