Canonical Allele Identifier: PA916019173
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 540611
ClinVar RCV Id: RCV000650707 RCV002440358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Ala99Thr
CA10145271
NM_001301339.2:c.295G>A