Canonical Allele Identifier: PA2825648537
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496754
ClinVar RCV Id: RCV001992038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Ala71Ser
CA410265315
NM_001127649.3:c.211G>T