Canonical Allele Identifier: PA2573080290
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Val85Ile
CA133444
NM_001393500.2:c.253G>A