Canonical Allele Identifier: PA2580420952
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1712552
ClinVar RCV Id: RCV002300724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Met1239Val
CA344039194
NM_018136.5:c.3715A>G