Canonical Allele Identifier: PA645433975
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 365657
ClinVar RCV Id: RCV000340168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Met365Thr
CA5313313
NM_000787.4:c.1094T>C