Canonical Allele Identifier: PA207910
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 212722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2853Gln
CA207909
NM_018136.5:c.8558G>A