Canonical Allele Identifier: PA2573080288
Gene: TOMT HGNC NCBI
ClinVar RCV:
RCV000000575
ClinVar Variation:
545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Glu77Lys
CA251498
NM_001393500.2:c.229G>A