Canonical Allele Identifier: PA2829883989
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2300142
ClinVar RCV Id: RCV002878464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His2263Arg
CA344021485
NM_018136.5:c.6788A>G