Canonical Allele Identifier: PA2826287684
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 764935
ClinVar RCV Id: RCV000943303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Arg1506His
CA1309001
NM_001206846.2:c.4517G>A