Canonical Allele Identifier: PA2826594708
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Gly301Arg
CA3122544
NM_001281738.1:c.901G>A
CA358562319
NM_001281738.1:c.901G>C