Canonical Allele Identifier: PA645394996
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294627
ClinVar RCV Id: RCV000391415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His1700Tyr
CA1309812
NM_018136.5:c.5098C>T