Canonical Allele Identifier: PA2580421033
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1907662
ClinVar RCV Id: RCV002580961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Gln2205Lys
CA1309558
NM_018136.5:c.6613C>A