ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826146847
Gene: PEX11B
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000594227
RCV000952299
RCV003980095
ClinVar Variation:
500524
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171724.1:p.Cys139Tyr
CA1055607
NM_001184795.1:c.416G>A