Canonical Allele Identifier: PA916062320
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 735069
ClinVar RCV Id: RCV000910559 RCV001098623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Asp578Asn
CA1310658
NM_018136.5:c.1732G>A