Canonical Allele Identifier: PA2580421002
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2284519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser1833Thr
CA1309745
NM_018136.5:c.5497T>A