Allele Registry

Canonical Allele Identifier: PA110876

Gene: DBH HGNC NCBI

ClinVar RCV:

RCV000201811

ClinVar Variation:

217764

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Asp345Asn	CA347616 NM_000787.4:c.1033G>A