Canonical Allele Identifier: PA2829571747
Gene: PEX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 956787
ClinVar RCV Id: RCV001229660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004804.2:p.Val313Ile
CA5959758
NM_004813.4:c.937G>A