Canonical Allele Identifier: PA891855644
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 585447
ClinVar RCV Id: RCV000710635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val169Ile
CA344020471
NM_018136.5:c.505G>A