Canonical Allele Identifier: PA109833
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 12326
ClinVar RCV Id: RCV000013119 RCV000622283
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Thr494Met
CA278130
NM_199292.3:c.1481C>T