Allele Registry

Canonical Allele Identifier: PA106241

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000024296

RCV003226168

ClinVar Variation:

31590

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153695.1:p.Arg199Cys	CA129827 NM_001160223.2:c.595C>T