Canonical Allele Identifier: PA2826594275
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 431962
ClinVar RCV Id: RCV000498882 RCV000763115 RCV001266160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Leu77Arg
CA3122353
NM_001281738.1:c.230T>G