Canonical Allele Identifier: PA645394731
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Leu65Met
CA1310947
NM_018136.5:c.193C>A