Canonical Allele Identifier: PA2573217096
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1443179
ClinVar RCV Id: RCV001953371 RCV003170071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.His81Tyr
CA6168590
NM_001393500.2:c.241C>T