Canonical Allele Identifier: PA2826287566
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1029519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Gly1228Asp
CA35883345
NM_001206846.2:c.3683G>A