Canonical Allele Identifier: PA2826287214
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 975502
ClinVar RCV Id: RCV001252165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Glu254Gly
CA1310814
NM_001206846.2:c.761A>G