Canonical Allele Identifier: PA2826594644
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2511021
ClinVar RCV Id: RCV003244087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Val264Phe
CA312537
NM_001281738.1:c.790G>T