Canonical Allele Identifier: PA2829201974
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2326892
ClinVar RCV Id: RCV002921133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Arg21Trp
CA6168571
NM_001393500.2:c.61C>T