Canonical Allele Identifier: PA2826287528
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2054383
ClinVar RCV Id: RCV002927952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser1110Gly
CA1310201
NM_001206846.2:c.3328A>G