Canonical Allele Identifier: PA2573198059
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429139
ClinVar RCV Id: RCV001938780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Gln94Glu
CA410915340
NM_001301339.2:c.280C>G