Canonical Allele Identifier: PA658801092
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 529773
ClinVar RCV Id: RCV000635253 RCV003905708 RCV003151800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Gly482Arg
CA5313546
NM_000787.4:c.1444G>A
CA375420766
NM_000787.4:c.1444G>C