Canonical Allele Identifier: PA2825151592
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2495488
ClinVar RCV Id: RCV003213606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Glu234Lys
CA379127168
NM_000360.3:c.700G>A