Allele Registry

Canonical Allele Identifier: PA915988686

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000049644

RCV001090583

RCV002273950

RCV003492394

ClinVar Variation:

56232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158183.1:p.Lys95_Leu99del	CA263575 NM_001164711.2:c.284_298del