Canonical Allele Identifier: PA913198642
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 595524
ClinVar RCV Id: RCV000731090 RCV000898569 RCV003453528 RCV003918204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Lys1862Glu
CA1309729
NM_018136.5:c.5584A>G