Canonical Allele Identifier: PA2829202045
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 228842
ClinVar RCV Id: RCV000219698 RCV000341492 RCV000992285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.His235Tyr
CA6168646
NM_001393500.2:c.703C>T