Canonical Allele Identifier: PA645395133
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294608
ClinVar RCV Id: RCV000389834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2659Lys
CA10608702
NM_018136.5:c.7976G>A