Canonical Allele Identifier: PA645395094
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294615
ClinVar RCV Id: RCV000340582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile2246Val
CA10608706
NM_018136.5:c.6736A>G