Allele Registry

Canonical Allele Identifier: PA916058137

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000118187

RCV002247499

ClinVar Variation:

130158

HGVS (amino-acid)	Matching Registered Transcripts
NP_112216.3:p.Ile214Val	CA154972 NM_030954.4:c.640A>G