Canonical Allele Identifier: PA2826287659
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_001193775.1:p.His1454Asp
CA344007698
NM_001206846.2:c.4360C>G