Allele Registry

Canonical Allele Identifier: PA2825423257

Gene: RARG HGNC NCBI

ClinVar RCV:

RCV001690475

ClinVar Variation:

1277170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001036193.1:p.Ser416Leu	CA6596102 NM_001042728.3:c.1247C>T