Allele Registry

Canonical Allele Identifier: PA2825946644

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000024296

RCV003226168

ClinVar Variation:

31590

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153697.1:p.Arg115Cys	CA129827 NM_001160225.2:c.343C>T