Canonical Allele Identifier: PA2825151709
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1357568
ClinVar RCV Id: RCV001894009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Val275Gly
CA379126547
NM_000360.3:c.824T>G