Canonical Allele Identifier: PA1139737125
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 874104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr1082Ala
CA1310216
NM_018136.5:c.3244A>G