Canonical Allele Identifier: PA1139737297
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 876853
ClinVar RCV Id: RCV001102098 RCV001856395 RCV002556051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile1662Ser
CA1309830
NM_018136.5:c.4985T>G