Canonical Allele Identifier: PA2826593770
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_001268666.1:p.Gly425Arg
CA3122617
NM_001281737.2:c.1273G>A
CA358564526
NM_001281737.2:c.1273G>C