Allele Registry

Canonical Allele Identifier: PA2741845944

Gene: CHAD HGNC NCBI

ClinVar Allele:

2710795

ClinVar RCV:

RCV004308724

ClinVar Variation:

2535215

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258.2:p.Arg313Trp	CA8648264 NM_001267.3:c.937C>T