Canonical Allele Identifier: PA103020
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153
ClinVar RCV Id: RCV000002236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Gly89Arg
CA115369
NM_001127649.3:c.265G>A
CA410265631
NM_001127649.3:c.265G>C