Canonical Allele Identifier: PA2826612008
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 357640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265595.1:p.Gly207Ser
CA3873742
NM_001278666.2:c.619G>A