Canonical Allele Identifier: PA1139680941
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 837428
ClinVar RCV Id: RCV001038760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Leu317Phe
CA375415311
NM_000787.4:c.949C>T