Canonical Allele Identifier: PA2825648695
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 95879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Ala243Val
CA223512
NM_001127649.3:c.728C>T