Canonical Allele Identifier: PA285629
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 95072
ClinVar RCV Id: RCV000081077 RCV000174102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Pro456Leu
CA285628
NM_004453.4:c.1367C>T