Canonical Allele Identifier: PA658655148
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 444242
ClinVar RCV Id: RCV000513281 RCV001103470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Ala23Thr
CA5818873
NM_199292.3:c.67G>A