Canonical Allele Identifier: PA2580421009
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2179842
ClinVar RCV Id: RCV002599349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1891Gln
CA1309711
NM_018136.5:c.5672G>A