Canonical Allele Identifier: PA2826287674
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2500608
ClinVar RCV Id: RCV003225520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ala1480Asp
CA344007131
NM_001206846.2:c.4439C>A