Canonical Allele Identifier: PA2741966095
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2510892
ClinVar RCV Id: RCV003240316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile1904Val
CA1309698
NM_018136.5:c.5710A>G