Canonical Allele Identifier: PA2741854059
Gene: CHCHD10 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Cys129Arg
CA10145253
NM_001301339.2:c.385T>C