Canonical Allele Identifier: PA2499304252
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1009280
ClinVar RCV Id: RCV001306745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Thr342Ala
CA216284979
NM_199292.3:c.1024A>G