Canonical Allele Identifier: PA109487
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 553311
ClinVar RCV Id: RCV000668727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Ala241Thr
CA379128003
NM_199292.3:c.721G>A