Canonical Allele Identifier: PA2826780734
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 88762
ClinVar RCV Id: RCV000074412 RCV000478782 RCV000624675 RCV003398657
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277205.1:p.Arg275Cys
CA145343
NM_001290276.1:c.823C>T