Canonical Allele Identifier: PA2826287316
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294652
ClinVar RCV Id: RCV000331848 RCV001850514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Glu561Lys
CA1310671
NM_001206846.2:c.1681G>A