Canonical Allele Identifier: PA2829974984
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_067075.1:p.Ala152Thr
CA10635667
NM_021252.5:c.454G>A