Canonical Allele Identifier: PA2825648511
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2112298
ClinVar RCV Id: RCV003024255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Leu49Val
CA410264873
NM_001127649.3:c.145C>G