Canonical Allele Identifier: PA2826287215
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1918118
ClinVar RCV Id: RCV002617183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Asn260Lys
CA1310812
NM_001206846.2:c.780T>G
CA344019123
NM_001206846.2:c.780T>A