Allele Registry

Canonical Allele Identifier: PA2826307375

Gene: RNF146 HGNC NCBI

ClinVar RCV:

RCV004134048

ClinVar Variation:

2281465

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229778.1:p.Ser347Tyr	CA365588630 NM_001242849.2:c.1040C>A