Canonical Allele Identifier: PA2825151708
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1505895
ClinVar RCV Id: RCV001999635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Val275Ile
CA5818478
NM_000360.3:c.823G>A