ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826146845
Gene: PEX11B
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV001241766
ClinVar Variation:
966964
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171724.1:p.Ser136Pro
CA1055605
NM_001184795.1:c.406T>C