Canonical Allele Identifier: PA2826287774
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 874778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Val1751Ile
CA35861110
NM_001206846.2:c.5251G>A