Canonical Allele Identifier: PA2573272124
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1461980
ClinVar RCV Id: RCV001985585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr3040Asp
CA344007682
NM_018136.5:c.9118T>G