Canonical Allele Identifier: PA2499242997
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 299818
ClinVar RCV Id: RCV000370517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243339.1:p.Asp129His
CA10635306
NM_001256410.2:c.385G>C