Canonical Allele Identifier: PA1139737517
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 874778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val3336Ile
CA35861110
NM_018136.5:c.10006G>A