Canonical Allele Identifier: PA2741966243
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2909795
ClinVar RCV Id: RCV003732440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr2722Cys
CA1309279
NM_018136.5:c.8165A>G