Canonical Allele Identifier: PA2826001012
Gene: AMT HGNC NCBI
ClinVar RCV:
RCV000373179
ClinVar Variation:
346031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Asn231Lys
CA2398230
NM_001164710.2:c.693T>A
CA352789767
NM_001164710.2:c.693T>G