Canonical Allele Identifier: PA2826612237
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 357642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265597.1:p.Glu179Ala
CA3873782
NM_001278668.2:c.536A>C