Allele Registry

Canonical Allele Identifier: PA209609

Gene: ASPM HGNC NCBI

ClinVar RCV:

RCV000145155

RCV000195047

RCV000710082

ClinVar Variation:

157844

HGVS (amino-acid)	Matching Registered Transcripts
NP_060606.3:p.Met1983Leu	CA209608 NM_018136.5:c.5947A>T CA344024013 NM_018136.5:c.5947A>C