Allele Registry

Canonical Allele Identifier: PA2826329680

Gene: RARG HGNC NCBI

ClinVar RCV:

RCV001690475

ClinVar Variation:

1277170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230660.1:p.Ser306Leu	CA6596102 NM_001243731.2:c.917C>T