Canonical Allele Identifier: PA1139737268
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 876854
ClinVar RCV Id: RCV001102099 RCV001552844 RCV003945810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val1659Phe
CA1309833
NM_018136.5:c.4975G>T