Canonical Allele Identifier: PA2573272097
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1444352
ClinVar RCV Id: RCV001982362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala2863Ser
CA344012203
NM_018136.5:c.8587G>T