Canonical Allele Identifier: PA2580297600
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 2131408
ClinVar RCV Id: RCV003052436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003837.1:p.Asp217Tyr
CA342120677
NM_003846.3:c.649G>T