Canonical Allele Identifier: PA891855668
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 585442
ClinVar RCV Id: RCV000710624 RCV003453511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg601Ile
CA1310649
NM_018136.5:c.1802G>T