Canonical Allele Identifier: PA2826287581
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294635
ClinVar RCV Id: RCV000388841 RCV000946545 RCV001252172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Arg1264His
CA1310078
NM_001206846.2:c.3791G>A