Canonical Allele Identifier: PA2826393577
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 299818
ClinVar RCV Id: RCV000370517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243340.1:p.Asp100His
CA10635306
NM_001256411.2:c.298G>C