Allele Registry

Canonical Allele Identifier: PA347657

Gene: DBH HGNC NCBI

ClinVar RCV:

RCV000201835

ClinVar Variation:

217763

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Cys269Phe	CA347656 NM_000787.4:c.806G>T