Canonical Allele Identifier: PA2580573260
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897589
ClinVar RCV Id: RCV002572099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998885.1:p.Arg15Cys
CA410917079
NM_213720.3:c.43C>T