Allele Registry

Canonical Allele Identifier: PA100756

Gene: EHHADH HGNC NCBI

ClinVar RCV:

RCV000082871

ClinVar Variation:

96711

HGVS (amino-acid)	Matching Registered Transcripts
NP_001957.2:p.Glu3Lys	CA149692 NM_001966.4:c.7G>A