Canonical Allele Identifier: PA154824
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 130059
ClinVar RCV Id: RCV000118086 RCV000385619 RCV000878180 RCV003975035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067075.1:p.Ala198Thr
CA154823
NM_021252.5:c.592G>A