Canonical Allele Identifier: PA271074
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157846
ClinVar RCV Id: RCV000145158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Asn201Asp
CA271073
NM_018136.5:c.601A>G