Canonical Allele Identifier: PA2826146910
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1387218
ClinVar RCV Id: RCV001905982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Thr235Asn
CA342120281
NM_001184795.1:c.704C>A