Canonical Allele Identifier: PA2826779155
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 2430936
ClinVar RCV Id: RCV003129469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277146.1:p.Leu171Pro
CA351886301
NM_001290217.2:c.512T>C