Canonical Allele Identifier: PA2580421069
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2047895
ClinVar RCV Id: RCV002918387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Met2752Ile
CA344013772
NM_018136.5:c.8256G>T
CA344013773
NM_018136.5:c.8256G>C
CA344013774
NM_018136.5:c.8256G>A