Canonical Allele Identifier: PA2573272178
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1388732
ClinVar RCV Id: RCV001886815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala3386Pro
CA343997247
NM_018136.5:c.10156G>C