Canonical Allele Identifier: PA916062567
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 640410
ClinVar RCV Id: RCV001103469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Lys24Arg
CA5818872
NM_199293.3:c.71A>G