Canonical Allele Identifier: PA2829202048
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 163944
ClinVar RCV Id: RCV000150999 RCV002051818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Ile249Leu
CA176674
NM_001393500.2:c.745A>C
CA381727444
NM_001393500.2:c.745A>T