Canonical Allele Identifier: PA2580420944
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2227480
ClinVar RCV Id: RCV002678800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr1172Met
CA1310152
NM_018136.5:c.3515C>T