Canonical Allele Identifier: PA645433963
Gene: DBH HGNC NCBI

Linked Data

ClinVar Variation Id: 365636
ClinVar RCV Id: RCV000385719 RCV004022110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000778.3:p.Val136Ala
CA10626766
NM_000787.4:c.407T>C