Allele Registry

Canonical Allele Identifier: PA341157

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000012756

RCV003230355

ClinVar Variation:

11976

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158182.1:p.His42Arg	CA341155 NM_001164710.2:c.125A>G