Canonical Allele Identifier: PA2573080287
Gene: TOMT HGNC NCBI
ClinVar RCV:
RCV000000574
ClinVar Variation:
544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Trp72Arg
CA251497
NM_001393500.2:c.214T>C
CA381718166
NM_001393500.2:c.214T>A