Canonical Allele Identifier: PA2580421076
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1806357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr2872Met
CA1309188
NM_018136.5:c.8615C>T