Canonical Allele Identifier: PA2573271914
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1507876
ClinVar RCV Id: RCV002009603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1681Thr
CA1309823
NM_018136.5:c.5041G>A