Canonical Allele Identifier: PA2741966245
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2572355
ClinVar RCV Id: RCV003314240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Phe2735Ser
CA344013879
NM_018136.5:c.8204T>C