Canonical Allele Identifier: PA2573271912
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1481514
ClinVar RCV Id: RCV002022311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile1655Ser
CA1309836
NM_018136.5:c.4964T>G