Allele Registry

Canonical Allele Identifier: PA2826307358

Gene: RNF146 HGNC NCBI

ClinVar RCV:

RCV004134048

ClinVar Variation:

2281465

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229777.1:p.Ser346Tyr	CA365588630 NM_001242848.2:c.1037C>A