ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA1139694893
Gene: RARB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001089954
ClinVar Variation:
870386
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001277145.1:p.Phe286Val
CA351886271
NM_001290216.3:c.856T>G