Canonical Allele Identifier: PA645463600
Gene: ETFDH HGNC NCBI
ClinVar RCV:
RCV000392282
ClinVar Variation:
347957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Ile48Val
CA3122283
NM_004453.4:c.142A>G