Allele Registry

Canonical Allele Identifier: PA154973

Gene: RNF170 HGNC NCBI

ClinVar RCV:

RCV000118187

RCV002247499

ClinVar Variation:

130158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153695.1:p.Ile214Val	CA154972 NM_001160223.2:c.640A>G