Canonical Allele Identifier: PA645395250
Gene: ASPM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg3308Leu
CA16044274
NM_018136.5:c.9923G>T