Canonical Allele Identifier: PA2826001108
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 531761
ClinVar RCV Id: RCV000638268 RCV001090580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg327His
CA2398140
NM_001164710.2:c.980G>A