Canonical Allele Identifier: PA342238
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21572
ClinVar RCV Id: RCV000020762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Gly1028Arg
CA342237
NM_018136.5:c.3082G>A
CA344044625
NM_018136.5:c.3082G>C