Canonical Allele Identifier: PA271064
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157837
ClinVar RCV Id: RCV000145148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr1861Cys
CA271063
NM_018136.5:c.5582A>G