Allele Registry

Canonical Allele Identifier: PA263577

Gene: AMT HGNC NCBI

ClinVar RCV:

RCV000049644

RCV001090583

RCV002273950

RCV003492394

ClinVar Variation:

56232

HGVS (amino-acid)	Matching Registered Transcripts
NP_000472.2:p.Lys151_Leu155del	CA263575 NM_000481.4:c.452_466del