Canonical Allele Identifier: PA207594
Gene: RAB23 HGNC NCBI

Linked Data

ClinVar Variation Id: 211976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057361.3:p.Ala73Val
CA207593
NM_016277.5:c.218C>T