Canonical Allele Identifier: PA2825151836
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1347764
ClinVar RCV Id: RCV002050674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Gln346His
CA5818409
NM_000360.3:c.1038G>C
CA379125941
NM_000360.3:c.1038G>T