Canonical Allele Identifier: PA2826001555
Gene: AMT HGNC NCBI
ClinVar RCV:
RCV000049643
ClinVar Variation:
56231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158184.1:p.Asn145Ile
CA263573
NM_001164712.2:c.434A>T