Canonical Allele Identifier: PA2826287220
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21616
ClinVar RCV Id: RCV000020806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser283Phe
CA342282
NM_001206846.2:c.848C>T