Canonical Allele Identifier: PA351298
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 242522
ClinVar RCV Id: RCV001381020
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Leu496Pro
CA351297
NM_004453.4:c.1487T>C