Canonical Allele Identifier: PA2826612061
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 211976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265596.1:p.Ala73Val
CA207593
NM_001278667.2:c.218C>T