Canonical Allele Identifier: PA2580420993
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2104291
ClinVar RCV Id: RCV003031309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1667Phe
CA2580061891
NM_018136.5:c.4999_5000delinsTT