Canonical Allele Identifier: PA645394912
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 388993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1258Thr
CA1310080
NM_018136.5:c.3772G>A