Allele Registry

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Canonical Allele Identifier: PA2825151593

Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2147774

ClinVar RCV Id: RCV003068517

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Glu234Asp	CA379127153 NM_000360.3:c.702G>T CA379127154 NM_000360.3:c.702G>C