Canonical Allele Identifier: PA2830434491
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 493087
ClinVar RCV Id: RCV000585047 RCV002530832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Arg60Gln
CA216227842
NM_199293.3:c.179G>A