Allele Registry

Canonical Allele Identifier: PA270988

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000145070

RCV000267551

RCV000907315

RCV003965090

ClinVar Variation:

157769

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Thr336Lys	CA270987 NM_018136.5:c.1007C>A