Canonical Allele Identifier: PA2826146900
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 2050803
ClinVar RCV Id: RCV002922089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Gly217Ser
CA342120501
NM_001184795.1:c.649G>A