Allele Registry

Canonical Allele Identifier: PA104373

Gene: AMELX HGNC NCBI

ClinVar RCV:

RCV000011890

ClinVar Variation:

11140

HGVS (amino-acid)	Matching Registered Transcripts
NP_001133.1:p.Thr37Ile	CA121369 NM_001142.2:c.110C>T