Canonical Allele Identifier: PA658830305
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 546656
ClinVar RCV Id: RCV000658581
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Pro355Leu
CA379126102
NM_199292.3:c.1064C>T