Allele Registry

Canonical Allele Identifier: PA2826001120

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000224719

RCV000238619

RCV001084238

ClinVar Variation:

235658

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158182.1:p.Arg338Gln	CA2398133 NM_001164710.2:c.1013G>A