Canonical Allele Identifier: PA1139704037
Gene: PEX16 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004804.2:p.Gly336Arg
CA5959716
NM_004813.4:c.1006G>C