Canonical Allele Identifier: PA2573315015
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1440375
ClinVar RCV Id: RCV001967649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Thr269Met
CA5818512
NM_199292.3:c.806C>T