Canonical Allele Identifier: PA2580421011
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2473775
ClinVar RCV Id: RCV003197987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1900Asp
CA344024721
NM_018136.5:c.5699C>A