Canonical Allele Identifier: PA2830434672
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 586831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Val129Leu
CA5818730
NM_199293.3:c.385G>T
CA379112135
NM_199293.3:c.385G>C