Allele Registry

Canonical Allele Identifier: PA2580172183

Gene: CHAD HGNC NCBI

ClinVar RCV:

RCV004251701

ClinVar Variation:

2462344

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258.2:p.Ala198Thr	CA8648345 NM_001267.3:c.592G>A