Canonical Allele Identifier: PA2829883918
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 3130491
ClinVar RCV Id: RCV004420906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile2107Val
CA1309606
NM_018136.5:c.6319A>G