Canonical Allele Identifier: PA2830433244
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2150468
ClinVar RCV Id: RCV003067582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Ala11Thr
CA5818883
NM_199292.3:c.31G>A