Canonical Allele Identifier: PA2826287268
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2491019
ClinVar RCV Id: RCV003215636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Cys405Arg
CA1310752
NM_001206846.2:c.1213T>C