Canonical Allele Identifier: PA2825151656
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2808963
ClinVar RCV Id: RCV003625150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Phe255Leu
CA379126837
NM_000360.3:c.765T>G
CA379126840
NM_000360.3:c.765T>A
CA379126851
NM_000360.3:c.763T>C