Canonical Allele Identifier: PA2573271119
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375426
ClinVar RCV Id: RCV001879663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Thr7Ile
CA410264080
NM_017929.6:c.20C>T