Allele Registry

Canonical Allele Identifier: PA347666

Gene: DBH HGNC NCBI

ClinVar RCV:

RCV000201842

ClinVar Variation:

217766

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Tyr556Cys	CA347665 NM_000787.4:c.1667A>G