Canonical Allele Identifier: PA658674857
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 448684
ClinVar RCV Id: RCV000516963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Ala332Thr
CA5818450
NM_199292.3:c.994G>A