Canonical Allele Identifier: PA2826594393
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 418183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Ala126Val
CA3122394
NM_001281738.1:c.377C>T