Canonical Allele Identifier: PA2826000840
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2198317
ClinVar RCV Id: RCV002640389 RCV002629297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg62Trp
CA2398457
NM_001164710.2:c.184C>T