Canonical Allele Identifier: PA2825648502
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2065411
ClinVar RCV Id: RCV002958453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Ala41Thr
CA410264690
NM_001127649.3:c.121G>A