Allele Registry

Canonical Allele Identifier: PA2826780474

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277195.1:p.Phe230Val	CA351886271 NM_001290266.2:c.688T>G