Canonical Allele Identifier: PA2580420875
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2204422
ClinVar RCV Id: RCV002644562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val266Ile
CA1310809
NM_018136.5:c.796G>A