Canonical Allele Identifier: PA2826594853
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 95072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Pro395Leu
CA285628
NM_001281738.1:c.1184C>T