Canonical Allele Identifier: PA2580421005
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1805120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr1867Lys
CA1309726
NM_018136.5:c.5600C>A