Canonical Allele Identifier: PA2580420994
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1937830
ClinVar RCV Id: RCV002627767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1667Cys
CA1309827
NM_018136.5:c.4999C>T