Allele Registry

Canonical Allele Identifier: PA2826780708

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277205.1:p.Phe167Val	CA351886271 NM_001290276.1:c.499T>G