Canonical Allele Identifier: PA2826240882
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186248.1:p.Arg98Trp
CA115367
NM_001199319.1:c.292C>T