Canonical Allele Identifier: PA2573272084
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1433831
ClinVar RCV Id: RCV001984460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2750Thr
CA344013789
NM_018136.5:c.8249G>C