Canonical Allele Identifier: PA2830435127
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2174771
ClinVar RCV Id: RCV002598987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Ala274Thr
CA379126968
NM_199293.3:c.820G>A