Canonical Allele Identifier: PA2825151598
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1303321
ClinVar RCV Id: RCV001757876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Tyr236Asp
CA379127126
NM_000360.3:c.706T>G