Canonical Allele Identifier: PA915988702
Gene: AMT HGNC NCBI
ClinVar RCV:
RCV000049638
ClinVar Variation:
56226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158184.1:p.Gly47Trp
CA263562
NM_001164712.2:c.139G>T