Canonical Allele Identifier: PA2826873343
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897589
ClinVar RCV Id: RCV002572099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Arg15Cys
CA410917079
NM_001301339.2:c.43C>T