Canonical Allele Identifier: PA2580421007
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2427887
ClinVar RCV Id: RCV003116858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Lys1875Glu
CA1309721
NM_018136.5:c.5623A>G