Canonical Allele Identifier: PA2829202027
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2442643
ClinVar RCV Id: RCV003149415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Glu196Lys
CA381724785
NM_001393500.2:c.586G>A