Canonical Allele Identifier: PA645395256
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 234723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr3353His
CA1308800
NM_018136.5:c.10057T>C