Canonical Allele Identifier: PA2826287513
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2193108
ClinVar RCV Id: RCV002623875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Thr1076Lys
CA1310221
NM_001206846.2:c.3227C>A