Canonical Allele Identifier: PA2826001388
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 346029
ClinVar RCV Id: RCV000330007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158183.1:p.Val265Met
CA2398193
NM_001164711.2:c.793G>A