Canonical Allele Identifier: PA093729
Gene: RAB33B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112586.1:p.Lys46Gln
CA143715
NM_031296.3:c.136A>C