Allele Registry

Canonical Allele Identifier: PA204470

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000190504

ClinVar Variation:

208491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153696.1:p.Gly164Arg	CA204469 NM_001160224.2:c.490G>A CA371110298 NM_001160224.2:c.490G>C