Canonical Allele Identifier: PA2826105198
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139589
ClinVar RCV Id: RCV000128530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Cys247Arg
CA163284
NM_001172086.2:c.739T>C