Allele Registry

Canonical Allele Identifier: PA2580448202

Gene: CHTF18 HGNC NCBI

ClinVar RCV:

RCV004225564

ClinVar Variation:

2392127

HGVS (amino-acid)	Matching Registered Transcripts
NP_071375.1:p.Arg389His	CA7795003 NM_022092.3:c.1166G>A