Canonical Allele Identifier: PA2830434777
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 304079
ClinVar RCV Id: RCV000487959 RCV000401042
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Arg160His
CA5818680
NM_199293.3:c.479G>A