Allele Registry

Canonical Allele Identifier: PA271080

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000145163

RCV000994210

ClinVar Variation:

157851

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Asn2044Ser	CA271079 NM_018136.5:c.6131A>G