Allele Registry

Canonical Allele Identifier: PA111460

Gene: CHCHD10 HGNC NCBI

ClinVar RCV:

RCV000192231

RCV000533214

RCV000990379

RCV001579805

RCV002433830

RCV003955119

RCV003993872

ClinVar Variation:

204291

HGVS (amino-acid)	Matching Registered Transcripts
NP_998885.1:p.Pro34Ser	CA347295 NM_213720.3:c.100C>T