Canonical Allele Identifier: PA2826287550
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2491903
ClinVar RCV Id: RCV003212960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser1185Cys
CA344040183
NM_001206846.2:c.3554C>G