Canonical Allele Identifier: PA913198636
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 594145
ClinVar RCV Id: RCV000729363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1667His
CA1309826
NM_018136.5:c.5000G>A