Canonical Allele Identifier: PA2826146894
Gene: PEX11B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Pro207Arg
CA342120609
NM_001184795.1:c.620C>G