Canonical Allele Identifier: PA2826287297
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1501370
ClinVar RCV Id: RCV002042798 RCV003303615 RCV003453950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ile492Val
CA1310704
NM_001206846.2:c.1474A>G