Canonical Allele Identifier: PA645394889
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 379166
ClinVar RCV Id: RCV000436883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile1083Val
CA1310215
NM_018136.5:c.3247A>G