Canonical Allele Identifier: PA916017489
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 88762
ClinVar RCV Id: RCV000074412 RCV000478782 RCV000624675 RCV003398657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277145.1:p.Arg394Cys
CA145343
NM_001290216.3:c.1180C>T