Canonical Allele Identifier: PA2580421057
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1955028
ClinVar RCV Id: RCV002690380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Cys2635Tyr
CA1309319
NM_018136.5:c.7904G>A