Canonical Allele Identifier: PA1139680940
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 835077
ClinVar RCV Id: RCV001035885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Gly316Ser
CA5313250
NM_000787.4:c.946G>A