Allele Registry

Canonical Allele Identifier: PA2580172185

Gene: CHAD HGNC NCBI

ClinVar RCV:

RCV004211508

ClinVar Variation:

2378108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258.2:p.Gly266Ser	CA8648301 NM_001267.3:c.796G>A