Canonical Allele Identifier: PA2826780472
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 862649
ClinVar RCV Id: RCV001069406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277195.1:p.Arg220Thr
CA351886200
NM_001290266.2:c.659G>C