Canonical Allele Identifier: PA2573271726
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1521033
ClinVar RCV Id: RCV002031059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Met404Thr
CA344017187
NM_018136.5:c.1211T>C