Canonical Allele Identifier: PA2825151834
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1913004
ClinVar RCV Id: RCV002593546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Phe344Leu
CA379125954
NM_000360.3:c.1032C>G
CA379125955
NM_000360.3:c.1032C>A
CA379125960
NM_000360.3:c.1030T>C