Canonical Allele Identifier: PA658673902
Gene: ETFDH HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Pro227Thr
CA3122427
NM_004453.4:c.679C>A