Canonical Allele Identifier: PA916062930
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 681103
ClinVar RCV Id: RCV000840947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Gln2795Glu
CA1309235
NM_018136.5:c.8383C>G