Canonical Allele Identifier: PA2830435153
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2808963
ClinVar RCV Id: RCV003625150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Phe282Leu
CA379126837
NM_199293.3:c.846T>G
CA379126840
NM_199293.3:c.846T>A
CA379126851
NM_199293.3:c.844T>C