Canonical Allele Identifier: PA2826780483
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 1309156
ClinVar RCV Id: RCV001765325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277195.1:p.His242Pro
CA351886355
NM_001290266.2:c.725A>C
CA2573052133
NM_001290266.2:c.725_726delinsCA