Canonical Allele Identifier: PA2826287737
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 434404
ClinVar RCV Id: RCV000503336 RCV000727279 RCV001099802 RCV003258831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Cys1641Gly
CA1308881
NM_001206846.2:c.4921T>G