Allele Registry

Canonical Allele Identifier: PA2826619307

Gene: RNF19A HGNC NCBI

ClinVar RCV:

RCV004084401

ClinVar Variation:

2224182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267468.1:p.Met555Val	CA4828054 NM_001280539.2:c.1663A>G