Canonical Allele Identifier: PA2825151712
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1948864
ClinVar RCV Id: RCV002685854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Ser276Tyr
CA379126540
NM_000360.3:c.827C>A