Canonical Allele Identifier: PA2741966342
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2967321
ClinVar RCV Id: RCV003823999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ile3345Lys
CA343998535
NM_018136.5:c.10034T>A