Canonical Allele Identifier: PA312522
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 203711
ClinVar RCV Id: RCV000185888 RCV000297924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Thr31Ala
CA312521
NM_004453.4:c.91A>G