Canonical Allele Identifier: PA201673
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 195337
ClinVar RCV Id: RCV000175899 RCV000224312 RCV001085384 RCV001137939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Leu44Phe
CA201672
NM_017929.6:c.130C>T