Canonical Allele Identifier: PA2580297601
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 2008702
ClinVar RCV Id: RCV002816662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003837.1:p.Pro221Arg
CA342120609
NM_003846.3:c.662C>G