Allele Registry

Canonical Allele Identifier: PA2826001270

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000549987

RCV000991518

RCV001573069

ClinVar Variation:

462898

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158183.1:p.Glu155Lys	CA2398296 NM_001164711.2:c.463G>A