Canonical Allele Identifier: PA2825229352
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 862649
ClinVar RCV Id: RCV001069406
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000956.2:p.Arg269Thr
CA351886200
NM_000965.5:c.806G>C