Allele Registry

Canonical Allele Identifier: PA915988793

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000049651

RCV000436156

ClinVar Variation:

56239

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158184.1:p.Arg296His	CA263586 NM_001164712.2:c.887G>A