Canonical Allele Identifier: PA171282
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21638
ClinVar RCV Id: RCV000020828 RCV000145240 RCV000514910 RCV003904856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His3258Arg
CA171281
NM_018136.5:c.9773A>G