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