Canonical Allele Identifier: PA2825151751
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2090085
ClinVar RCV Id: RCV003020732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Ala301Ser
CA379126253
NM_000360.3:c.901G>T