Allele Registry

Canonical Allele Identifier: PA256149

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000012755

RCV000622444

RCV003230354

ClinVar Variation:

11975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158184.1:p.Gly47Arg	CA256146 NM_001164712.2:c.139G>A CA352791256 NM_001164712.2:c.139G>C