Canonical Allele Identifier: PA2826287778
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 234723
ClinVar RCV Id: RCV000218238 RCV000763779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Tyr1768His
CA1308800
NM_001206846.2:c.5302T>C