Canonical Allele Identifier: PA645433985
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 365677
ClinVar RCV Id: RCV000343761 RCV002524590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Gly614Arg
CA5313730
NM_000787.4:c.1840G>A
CA375423196
NM_000787.4:c.1840G>C