Canonical Allele Identifier: PA101592
Gene: ETFB HGNC NCBI

Linked Data

ClinVar Variation Id: 16716
ClinVar RCV Id: RCV000018200 RCV001235936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001976.1:p.Arg164Gln
CA126841
NM_001985.3:c.491G>A