Allele Registry

Canonical Allele Identifier: PA645479462

Gene: CHD2 HGNC NCBI

ClinVar Variation Id: 422208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001262.3:p.Lys1605Thr	CA7748566 NM_001271.4:c.4814A>C