Canonical Allele Identifier: PA2826611985
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 417740
ClinVar RCV Id: RCV000477736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265595.1:p.Val161Leu
CA16616858
NM_001278666.2:c.481G>C