Canonical Allele Identifier: PA115368
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Arg98Trp
CA115367
NM_017929.6:c.292C>T