Canonical Allele Identifier: PA2573315027
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1505895
ClinVar RCV Id: RCV001999635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Val306Ile
CA5818478
NM_199292.3:c.916G>A