Canonical Allele Identifier: PA2830435087
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2495488
ClinVar RCV Id: RCV003213606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Glu261Lys
CA379127168
NM_199293.3:c.781G>A