Canonical Allele Identifier: PA2826873496
Gene: CHCHD10 HGNC NCBI
ClinVar RCV:
RCV001321552
ClinVar Variation:
1021740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Glu79Lys
CA410915910
NM_001301339.2:c.235G>A