Canonical Allele Identifier: PA2825151081
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 695326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Glu27Asp
CA5818870
NM_000360.3:c.81G>T
CA379112773
NM_000360.3:c.81G>C