Canonical Allele Identifier: PA2825460002
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073336.2:p.Trp250Arg
CA154235
NM_001079867.2:c.748T>C
CA371556670
NM_001079867.2:c.748T>A