Canonical Allele Identifier: PA1139707983
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 966964
ClinVar RCV Id: RCV001241766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003837.1:p.Ser150Pro
CA1055605
NM_003846.3:c.448T>C