Allele Registry

Canonical Allele Identifier: PA1139694893

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277145.1:p.Phe286Val	CA351886271 NM_001290216.3:c.856T>G