Canonical Allele Identifier: PA645395656
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_954986.2:p.Arg164His
CA5818680
NM_199292.3:c.491G>A