Allele Registry

Canonical Allele Identifier: PA2826593732

Gene: ETFDH HGNC NCBI

ClinVar Allele:

100972

ClinVar RCV:

RCV000081077

RCV000174102

ClinVar Variation:

95072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268666.1:p.Pro409Leu	CA285628 NM_001281737.2:c.1226C>T