Canonical Allele Identifier: PA658739659
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 493087
ClinVar RCV Id: RCV000585047 RCV002530832
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Arg64Gln
CA216227842
NM_199292.3:c.191G>A