Canonical Allele Identifier: PA101602
Gene: ETFB HGNC NCBI

Linked Data

ClinVar Variation Id: 16718
ClinVar RCV Id: RCV002513095 RCV004525856 RCV000018202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001976.1:p.Asp128Asn
CA126842
NM_001985.3:c.382G>A