Canonical Allele Identifier: PA1139695174
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 858122
ClinVar RCV Id: RCV001063928 RCV003380834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Gly95Glu
CA342123214
NM_001184795.1:c.284G>A