Allele Registry

Canonical Allele Identifier: PA2580448198

Gene: CHTF18 HGNC NCBI

ClinVar RCV:

RCV004129054

ClinVar Variation:

2277680

HGVS (amino-acid)	Matching Registered Transcripts
NP_071375.1:p.Asn301Ser	CA276557703 NM_022092.3:c.902A>G