Allele Registry

Canonical Allele Identifier: PA915988720

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000049641

RCV002274890

ClinVar Variation:

56229

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158184.1:p.Ser77Leu	CA263569 NM_001164712.2:c.230C>T