Allele Registry

Canonical Allele Identifier: PA2829855028

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_057236.1:p.Phe167Val	CA351886271 NM_016152.4:c.499T>G