Allele Registry

Canonical Allele Identifier: PA110864

Gene: DBH HGNC NCBI

ClinVar RCV:

RCV000001821

ClinVar Variation:

1751

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Asp114Glu	CA339913 NM_000787.4:c.342C>A CA375409069 NM_000787.4:c.342C>G