Canonical Allele Identifier: PA645395151
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 234260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Met2752Arg
CA1309254
NM_018136.5:c.8255T>G