Canonical Allele Identifier: PA103031
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Leu45Pro
CA115374
NM_001127649.3:c.134T>C