Allele Registry

Canonical Allele Identifier: PA2826001108

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000638268

RCV001090580

ClinVar Variation:

531761

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