Canonical Allele Identifier: PA2830530683
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2944997
ClinVar RCV Id: RCV003800651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998885.1:p.Cys122Arg
CA10145253
NM_213720.3:c.364T>C