Canonical Allele Identifier: PA915956498
Gene: ETFB HGNC NCBI

Linked Data

ClinVar Variation Id: 203700
ClinVar RCV Id: RCV000416208 RCV000809414 RCV002516967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014763.1:p.Val328Ile
CA312500
NM_001014763.1:c.982G>A