Canonical Allele Identifier: PA2825151799
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 546656
ClinVar RCV Id: RCV000658581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Pro324Leu
CA379126102
NM_000360.3:c.971C>T