Canonical Allele Identifier: PA2825151028
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 412031
ClinVar RCV Id: RCV001273892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Thr7Pro
CA5818889
NM_000360.3:c.19A>C