Canonical Allele Identifier: PA2826593792
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 31602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268666.1:p.Pro436Leu
CA129836
NM_001281737.2:c.1307C>T