Canonical Allele Identifier: PA2573272134
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1406527
ClinVar RCV Id: RCV001915867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser3054Thr
CA1309027
NM_018136.5:c.9160T>A