Canonical Allele Identifier: PA2826594353
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 418182
ClinVar RCV Id: RCV000485144 RCV002525759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Arg114Cys
CA3122387
NM_001281738.1:c.340C>T