Allele Registry

Canonical Allele Identifier: PA2826781327

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277229.1:p.Phe236Val	CA351886271 NM_001290300.2:c.706T>G