Canonical Allele Identifier: PA2825151345
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 304079
ClinVar RCV Id: RCV000487959 RCV000401042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Arg133His
CA5818680
NM_000360.3:c.398G>A