Canonical Allele Identifier: PA2826001297
Gene: AMT HGNC NCBI
ClinVar RCV:
RCV000533799
ClinVar Variation:
462900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158183.1:p.Asp173His
CA352790066
NM_001164711.2:c.517G>C