Allele Registry

Canonical Allele Identifier: PA2825946645

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000118187

RCV002247499

ClinVar Variation:

130158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153697.1:p.Ile130Val	CA154972 NM_001160225.2:c.388A>G