Canonical Allele Identifier: PA2580420888
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2491019
ClinVar RCV Id: RCV003215636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Cys405Arg
CA1310752
NM_018136.5:c.1213T>C