Canonical Allele Identifier: PA2826594741
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 522495
ClinVar RCV Id: RCV000625637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Gly320Arg
CA358562756
NM_001281738.1:c.958G>C