Allele Registry

Canonical Allele Identifier: PA2826287338

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000371271

RCV001850513

ClinVar Variation:

294651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Pro609Ala	CA1310642 NM_001206846.2:c.1825C>G