Allele Registry

Canonical Allele Identifier: PA2580448210

Gene: CHTF18 HGNC NCBI

ClinVar RCV:

RCV004227290

ClinVar Variation:

2390020

HGVS (amino-acid)	Matching Registered Transcripts
NP_071375.1:p.Val442Met	CA394136579 NM_022092.3:c.1324G>A