Canonical Allele Identifier: PA2826393546
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 299820
ClinVar RCV Id: RCV000331024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243339.1:p.Ala181Thr
CA10635667
NM_001256410.2:c.541G>A