Allele Registry

Canonical Allele Identifier: PA915988696

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000638292

RCV003479181

RCV003937920

ClinVar Variation:

531783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158184.1:p.Arg34His	CA2398472 NM_001164712.2:c.101G>A