Canonical Allele Identifier: PA2580421003
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2095159
ClinVar RCV Id: RCV003013727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser1850Cys
CA344026323
NM_018136.5:c.5549C>G