Canonical Allele Identifier: PA2573235233
Gene: PEX11B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003837.1:p.Ser168Arg
CA342121262
NM_003846.3:c.504T>G
CA342121264
NM_003846.3:c.504T>A
CA342121274
NM_003846.3:c.502A>C