Allele Registry

Canonical Allele Identifier: PA2829599070

Gene: HADH HGNC NCBI

ClinVar RCV:

RCV002572591

ClinVar Variation:

1897761

HGVS (amino-acid)	Matching Registered Transcripts
NP_005318.6:p.His141Arg	CA3037474 NM_005327.7:c.422A>G