Canonical Allele Identifier: PA2580421006
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2471935
ClinVar RCV Id: RCV003202846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Thr1874Ala
CA35873594
NM_018136.5:c.5620A>G