Canonical Allele Identifier: PA2580566805
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2150468
ClinVar RCV Id: RCV003067582
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Ala11Thr
CA5818883
NM_199293.3:c.31G>A