Allele Registry

Canonical Allele Identifier: PA2826000942

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000549987

RCV000991518

RCV001573069

ClinVar Variation:

462898

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158182.1:p.Glu167Lys	CA2398296 NM_001164710.2:c.499G>A