Canonical Allele Identifier: PA2573271954
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1469792
ClinVar RCV Id: RCV001973102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1901Thr
CA1309704
NM_018136.5:c.5701G>A