Canonical Allele Identifier: PA2826001120
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 235658
ClinVar RCV Id: RCV000224719 RCV000238619 RCV001084238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg338Gln
CA2398133
NM_001164710.2:c.1013G>A