Canonical Allele Identifier: PA2826287672
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1367811
ClinVar RCV Id: RCV001964506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ile1478Met
CA1309019
NM_001206846.2:c.4434A>G