ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825229360
Gene: RARB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2430936
ClinVar RCV Id:
RCV003129469
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000956.2:p.Leu283Pro
CA351886301
NM_000965.5:c.848T>C