Canonical Allele Identifier: PA2830435212
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1948864
ClinVar RCV Id: RCV002685854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Ser303Tyr
CA379126540
NM_199293.3:c.908C>A