Allele Registry

Canonical Allele Identifier: PA891862585

Gene: CHCHD10 HGNC NCBI

ClinVar RCV:

RCV000693937

ClinVar Variation:

572533

HGVS (amino-acid)	Matching Registered Transcripts
NP_998885.1:p.Gly66Asp	CA410916186 NM_213720.3:c.197G>A