Canonical Allele Identifier: PA2825151412
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 526208
ClinVar RCV Id: RCV000764964 RCV003343960 RCV001766340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Val151Ala
CA5818661
NM_000360.3:c.452T>C