Canonical Allele Identifier: PA2580566806
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2188542
ClinVar RCV Id: RCV002620306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Phe14Leu
CA379112850
NM_199293.3:c.42C>G
CA379112851
NM_199293.3:c.42C>A
CA379112856
NM_199293.3:c.40T>C