Canonical Allele Identifier: PA2826594132
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 12028
ClinVar RCV Id: RCV000012808 RCV000224728 RCV000553294 RCV003231099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Ala23Thr
CA121817
NM_001281738.1:c.67G>A