Canonical Allele Identifier: PA2829202040
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2393789
ClinVar RCV Id: RCV002738691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Arg229His
CA224375652
NM_001393500.2:c.686G>A