Canonical Allele Identifier: PA2825229360
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 2430936
ClinVar RCV Id: RCV003129469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000956.2:p.Leu283Pro
CA351886301
NM_000965.5:c.848T>C