Canonical Allele Identifier: PA2826287746
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21638
ClinVar RCV Id: RCV000020828 RCV000145240 RCV000514910 RCV003904856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.His1673Arg
CA171281
NM_001206846.2:c.5018A>G