Canonical Allele Identifier: PA110876
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 217764
ClinVar RCV Id: RCV000201811
JSON-LD

Amino-acid Alleles

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