Canonical Allele Identifier: PA2825151517
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 304077
ClinVar RCV Id: RCV000289936 RCV000861197 RCV003930285
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Ile209Met
CA5818574
NM_000360.3:c.627C>G