Canonical Allele Identifier: PA2573271991
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1490826
ClinVar RCV Id: RCV001986071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His2112Arg
CA344023141
NM_018136.5:c.6335A>G