Canonical Allele Identifier: PA205315
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 210363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser311Arg
CA205314
NM_018136.5:c.933C>G
CA344018382
NM_018136.5:c.933C>A
CA344018392
NM_018136.5:c.931A>C