Canonical Allele Identifier: PA2499284109
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1041651
ClinVar RCV Id: RCV001345489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Gly14Arg
CA410264155
NM_017929.6:c.40G>A
CA410264156
NM_017929.6:c.40G>C