Canonical Allele Identifier: PA658818921
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 522495
ClinVar RCV Id: RCV000625637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Gly381Arg
CA358562756
NM_004453.4:c.1141G>C