Allele Registry

Canonical Allele Identifier: PA645433981

Gene: DBH HGNC NCBI

ClinVar RCV:

RCV000318690

RCV001653753

ClinVar Variation:

365671

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Arg549Cys	CA5313632 NM_000787.4:c.1645C>T