Canonical Allele Identifier: PA2830435123
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 12329
ClinVar RCV Id: RCV000013122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Thr272Pro
CA278132
NM_199293.3:c.814A>C