Canonical Allele Identifier: PA2826593732
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 95072

Amino-acid Alleles

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