Canonical Allele Identifier: PA645394808
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Glu561Lys
CA1310671
NM_018136.5:c.1681G>A