Canonical Allele Identifier: PA2573272076
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1506866
ClinVar RCV Id: RCV002038214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Gln2686His
CA1309294
NM_018136.5:c.8058A>C
CA344014200
NM_018136.5:c.8058A>T