Canonical Allele Identifier: PA2825151059
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2683131
ClinVar RCV Id: RCV003481998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Val18Met
CA5818876
NM_000360.3:c.52G>A