Canonical Allele Identifier: PA2826287793
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1388732
ClinVar RCV Id: RCV001886815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ala1801Pro
CA343997247
NM_001206846.2:c.5401G>C