Canonical Allele Identifier: PA1139755484
Gene: PEX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 956787
ClinVar RCV Id: RCV001229660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_476515.2:p.Val313Ile
CA5959758
NM_057174.3:c.937G>A