Canonical Allele Identifier: PA2825151550
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 374731
ClinVar RCV Id: RCV000416269 RCV000518710 RCV001833508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Pro218Leu
CA5818544
NM_000360.3:c.653C>T