Canonical Allele Identifier: PA2826594917
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459963
ClinVar RCV Id: RCV000554634 RCV001834766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Gly411Arg
CA3122617
NM_001281738.1:c.1231G>A
CA358564526
NM_001281738.1:c.1231G>C