Canonical Allele Identifier: PA916009431
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 299819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243341.1:p.Asp68Tyr
CA5452391
NM_001256412.2:c.202G>T