Canonical Allele Identifier: PA2829202025
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44041
ClinVar RCV Id: RCV000037016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Asp191Glu
CA133447
NM_001393500.2:c.573C>G
CA381724662
NM_001393500.2:c.573C>A