Canonical Allele Identifier: PA2826593580
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459962
ClinVar RCV Id: RCV000539322 RCV001829570 RCV003419931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268666.1:p.Gly315Arg
CA3122544
NM_001281737.2:c.943G>A
CA358562319
NM_001281737.2:c.943G>C