Allele Registry

Canonical Allele Identifier: PA2499234473

Gene: RARG HGNC NCBI

ClinVar Allele:

1265750

ClinVar RCV:

RCV001690475

ClinVar Variation:

1277170

HGVS (amino-acid)	Matching Registered Transcripts
NP_000957.1:p.Ser427Leu	CA6596102 NM_000966.6:c.1280C>T