Canonical Allele Identifier: PA2826287666
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1406527
ClinVar RCV Id: RCV001915867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser1469Thr
CA1309027
NM_001206846.2:c.4405T>A