Canonical Allele Identifier: PA2825151728
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 558576
ClinVar RCV Id: RCV000674870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Gly284Ser
CA379126405
NM_000360.3:c.850G>A