Canonical Allele Identifier: PA2826240775
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469588
ClinVar RCV Id: RCV001973056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186248.1:p.Pro18Ser
CA321284316
NM_001199319.1:c.52C>T