Canonical Allele Identifier: PA2830435327
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 12334
ClinVar RCV Id: RCV000013127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Cys355Phe
CA278134
NM_199293.3:c.1064G>T