Canonical Allele Identifier: PA2830435207
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1357568
ClinVar RCV Id: RCV001894009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Val302Gly
CA379126547
NM_199293.3:c.905T>G