Canonical Allele Identifier: PA2826240852
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496754
ClinVar RCV Id: RCV001992038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186248.1:p.Ala71Ser
CA410265315
NM_001199319.1:c.211G>T