Allele Registry

Canonical Allele Identifier: PA2826287712

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000020818

RCV000152802

RCV000710653

RCV001760667

ClinVar Variation:

21628

1307249

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Gln1595Pro	CA233487 NM_001206846.2:c.4784A>C CA2573051449 NM_001206846.2:c.4784_4785delinsCA