Canonical Allele Identifier: PA2580421065
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2296486
ClinVar RCV Id: RCV002877707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala2691Val
CA344014170
NM_018136.5:c.8072C>T