Canonical Allele Identifier: PA2829883769
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 3130483
ClinVar RCV Id: RCV004420898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Lys1716Asn
CA344027431
NM_018136.5:c.5148A>T
CA344027432
NM_018136.5:c.5148A>C