Allele Registry

Canonical Allele Identifier: PA102686

Gene: ETFA HGNC NCBI

ClinVar Allele:

17632

ClinVar RCV:

RCV000002711

RCV002281690

ClinVar Variation:

2593

HGVS (amino-acid)	Matching Registered Transcripts
NP_000117.1:p.Val157Gly	CA115637 NM_000126.4:c.470T>G