Canonical Allele Identifier: PA235292
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 180220
ClinVar RCV Id: RCV000157069 RCV000804540 RCV001731147 RCV002463652
ClinVar Variation Id: 1452852
ClinVar RCV Id: RCV002037768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Arg15Leu
CA235291
NM_001301339.2:c.44G>T
CA2573157754
NM_001301339.2:c.44_45delinsTT