Canonical Allele Identifier: PA109746
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1913004
ClinVar RCV Id: RCV002593546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Phe375Leu
CA379125954
NM_199292.3:c.1125C>G
CA379125955
NM_199292.3:c.1125C>A
CA379125960
NM_199292.3:c.1123T>C