Canonical Allele Identifier: PA2826594460
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459966
ClinVar RCV Id: RCV000558221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Pro166Thr
CA3122427
NM_001281738.1:c.496C>A