Canonical Allele Identifier: PA2829883979
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2133240
ClinVar RCV Id: RCV003040842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala2248Ser
CA344021619
NM_018136.5:c.6742G>T