Canonical Allele Identifier: PA2830433226
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2103686
ClinVar RCV Id: RCV003028930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Pro4Leu
CA379112908
NM_199292.3:c.11C>T