Allele Registry

Canonical Allele Identifier: PA113460

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000549987

RCV000991518

RCV001573069

ClinVar Variation:

462898

HGVS (amino-acid)	Matching Registered Transcripts
NP_000472.2:p.Glu211Lys	CA2398296 NM_000481.4:c.631G>A