Canonical Allele Identifier: PA2580421066
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2486071
ClinVar RCV Id: RCV003214719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val2728Ile
CA344013925
NM_018136.5:c.8182G>A