Canonical Allele Identifier: PA916062562
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 655788
ClinVar RCV Id: RCV001277079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Arg15Cys
CA5818882
NM_199293.3:c.43C>T