Canonical Allele Identifier: PA2829201993
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1706260
ClinVar RCV Id: RCV002284790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Ala57Pro
CA381717874
NM_001393500.2:c.169G>C