Canonical Allele Identifier: PA916062943
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 680363
ClinVar RCV Id: RCV000840137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr2852Cys
CA1309202
NM_018136.5:c.8555A>G