Canonical Allele Identifier: PA2826105203
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Trp250Arg
CA154235
NM_001172086.2:c.748T>C
CA371556670
NM_001172086.2:c.748T>A