Allele Registry

Canonical Allele Identifier: PA346135

Gene: CHCHD10 HGNC NCBI

ClinVar RCV:

RCV000157070

RCV001731148

ClinVar Variation:

180221

HGVS (amino-acid)	Matching Registered Transcripts
NP_998885.1:p.Gly66Val	CA346133 NM_213720.3:c.197G>T