Canonical Allele Identifier: PA2826611993
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 357642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265595.1:p.Glu179Ala
CA3873782
NM_001278666.2:c.536A>C