Canonical Allele Identifier: PA916062974
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 764935
ClinVar RCV Id: RCV000943303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg3091His
CA1309001
NM_018136.5:c.9272G>A