Canonical Allele Identifier: PA2580420996
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2072672
ClinVar RCV Id: RCV002967278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1713Cys
CA1309808
NM_018136.5:c.5137C>T