Canonical Allele Identifier: PA107791
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 30247
ClinVar RCV Id: RCV000023171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067075.1:p.Leu24Gln
CA129062
NM_021252.5:c.71T>A