Canonical Allele Identifier: PA658818228
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 522722
ClinVar RCV Id: RCV000625876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Lys1776Glu
CA344027006
NM_018136.5:c.5326A>G