Canonical Allele Identifier: PA2826594703
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 203721
ClinVar RCV Id: RCV000185898 RCV002282017 RCV002516968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Ala299Val
CA312541
NM_001281738.1:c.896C>T