Canonical Allele Identifier: PA2826594399
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 203715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Gly130Asp
CA312529
NM_001281738.1:c.389G>A