Canonical Allele Identifier: PA2826287350
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1939954
ClinVar RCV Id: RCV002658164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Lys639del
CA1310628
NM_001206846.2:c.1914_1916del