Canonical Allele Identifier: PA1139707983
Gene: PEX11B HGNC NCBI
ClinVar RCV:
RCV001241766
ClinVar Variation:
966964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003837.1:p.Ser150Pro
CA1055605
NM_003846.3:c.448T>C