Canonical Allele Identifier: PA2829201975
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 163941
ClinVar RCV Id: RCV000150998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.His22Gln
CA176672
NM_001393500.2:c.66C>G
CA381717244
NM_001393500.2:c.66C>A