Allele Registry

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Canonical Allele Identifier: PA2830435088

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_954987.2:p.Glu261Asp	CA379127153 NM_199293.3:c.783G>T CA379127154 NM_199293.3:c.783G>C