Canonical Allele Identifier: PA2826393613
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 130059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243341.1:p.Ala134Thr
CA154823
NM_001256412.2:c.400G>A