Canonical Allele Identifier: PA2826287574
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1899437
ClinVar RCV Id: RCV002575476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Asp1245Asn
CA1310102
NM_001206846.2:c.3733G>A