Canonical Allele Identifier: PA2826593370
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 203716
ClinVar RCV Id: RCV000185893 RCV001827992 RCV002517823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268666.1:p.Ala198Thr
CA312531
NM_001281737.2:c.592G>A