Canonical Allele Identifier: PA2829201977
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1339595
ClinVar RCV Id: RCV001824497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Arg25Gln
CA224374471
NM_001393500.2:c.74G>A