Allele Registry

Canonical Allele Identifier: PA915965297

Gene: DBH HGNC NCBI

ClinVar Variation Id: 639542

HGVS (amino-acid)	Matching Registered Transcripts
NP_000778.3:p.Phe516Leu	CA200981186 NM_000787.4:c.1546T>C CA375421083 NM_000787.4:c.1548C>A CA375421084 NM_000787.4:c.1548C>G