Canonical Allele Identifier: PA645395021
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294624
ClinVar RCV Id: RCV000375823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Gln1824del
CA1309750
NM_018136.5:c.5470_5472del