Canonical Allele Identifier: PA1139737416
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 874821
ClinVar RCV Id: RCV001098119 RCV001760071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Leu2736Val
CA1309265
NM_018136.5:c.8206T>G