Canonical Allele Identifier: PA2826594348
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 12029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Arg114Leu
CA121819
NM_001281738.1:c.341G>T