Canonical Allele Identifier: PA645395090
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294616
ClinVar RCV Id: RCV000393040 RCV002519462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Leu2239Pro
CA1309537
NM_018136.5:c.6716T>C