Canonical Allele Identifier: PA658818134
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 511337
ClinVar RCV Id: RCV000616569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val286Ala
CA344018745
NM_018136.5:c.857T>C