Canonical Allele Identifier: PA2830435112
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1516799
ClinVar RCV Id: RCV002026866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Tyr270His
CA379127025
NM_199293.3:c.808T>C