Canonical Allele Identifier: PA2573271953
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1494569
ClinVar RCV Id: RCV001989441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1886Cys
CA1309715
NM_018136.5:c.5656C>T