Canonical Allele Identifier: PA2826393542
Gene: RAB18 HGNC NCBI

Linked Data

ClinVar Variation Id: 299819
ClinVar RCV Id: RCV000275979 RCV002522156 RCV003480585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243339.1:p.Asp161Tyr
CA5452391
NM_001256410.2:c.481G>T