Canonical Allele Identifier: PA2826287668
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 3130505
ClinVar RCV Id: RCV004422902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ile1473Met
CA1309022
NM_001206846.2:c.4419C>G