Allele Registry

Canonical Allele Identifier: PA110886

Gene: DBH HGNC NCBI

ClinVar Allele:

16791

ClinVar RCV:

RCV000201816

ClinVar Variation:

217761

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Val101Met	CA347623 NM_000787.4:c.301G>A