Canonical Allele Identifier: PA645428536
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 281576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Ala10Val
CA10093193
NM_017929.6:c.29C>T