Canonical Allele Identifier: PA2580190964
Gene: CHCHD10 HGNC NCBI
ClinVar RCV:
RCV002780349
ClinVar Variation:
1980844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Cys139Tyr
CA410914091
NM_001301339.2:c.416G>A