Canonical Allele Identifier: PA2826146845
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 966964
ClinVar RCV Id: RCV001241766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Ser136Pro
CA1055605
NM_001184795.1:c.406T>C