Canonical Allele Identifier: PA1139736934
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_060606.3:p.Glu254Gly
CA1310814
NM_018136.5:c.761A>G