Canonical Allele Identifier: PA2826612229
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 417740
ClinVar RCV Id: RCV000477736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265597.1:p.Val161Leu
CA16616858
NM_001278668.2:c.481G>C