Canonical Allele Identifier: PA2825151824
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1363733
ClinVar RCV Id: RCV001905059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Pro337Leu
CA379125998
NM_000360.3:c.1010C>T