Canonical Allele Identifier: PA150634
Gene: RAB18 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067075.1:p.Thr95Arg
CA150633
NM_021252.5:c.284C>G