Canonical Allele Identifier: PA2580421092
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1717692
ClinVar RCV Id: RCV002297717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His3039Asp
CA344007698
NM_018136.5:c.9115C>G