Canonical Allele Identifier: PA2826287558
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2012864
ClinVar RCV Id: RCV002843432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Lys1195Arg
CA344040112
NM_001206846.2:c.3584A>G