Canonical Allele Identifier: PA2580420936
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2193108
ClinVar RCV Id: RCV002623875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr1076Lys
CA1310221
NM_018136.5:c.3227C>A