Canonical Allele Identifier: PA2826780707
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_001277205.1:p.Arg157Thr
CA351886200
NM_001290276.1:c.470G>C