Canonical Allele Identifier: PA2826287334
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2509058
ClinVar RCV Id: RCV003247271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Arg597Gly
CA344013413
NM_001206846.2:c.1789C>G