Canonical Allele Identifier: PA1139680982
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 912320
ClinVar RCV Id: RCV001165473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Leu328Arg
CA5313259
NM_000787.4:c.983T>G