Canonical Allele Identifier: PA2826612199
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 357644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265597.1:p.Ser101Ala
CA3873855
NM_001278668.2:c.301T>G