Canonical Allele Identifier: PA2580420992
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2126650
ClinVar RCV Id: RCV003047398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val1659Leu
CA35874131
NM_018136.5:c.4975G>C