Canonical Allele Identifier: PA312495
Gene: ETFB HGNC NCBI

Linked Data

ClinVar Variation Id: 203697
ClinVar RCV Id: RCV000185874 RCV000658852 RCV001086047 RCV001171332 RCV003907648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001976.1:p.Arg98Cys
CA312494
NM_001985.3:c.292C>T