Canonical Allele Identifier: PA2825151718
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1485307
ClinVar RCV Id: RCV002030373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Arg277Ser
CA379126529
NM_000360.3:c.829C>A