Canonical Allele Identifier: PA2580421030
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2184008
ClinVar RCV Id: RCV002627902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Met2116Lys
CA1309601
NM_018136.5:c.6347T>A