Allele Registry

Canonical Allele Identifier: PA645420139

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000224719

RCV000238619

RCV001084238

ClinVar Variation:

235658

HGVS (amino-acid)	Matching Registered Transcripts
NP_000472.2:p.Arg382Gln	CA2398133 NM_000481.4:c.1145G>A