Canonical Allele Identifier: PA2573315024
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1487677
ClinVar RCV Id: RCV002008748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Arg291Leu
CA216285419
NM_199292.3:c.872G>T