Allele Registry

Canonical Allele Identifier: PA2830415880

Gene: AMELX HGNC NCBI

ClinVar RCV:

RCV000011892

RCV001588809

ClinVar Variation:

11142

HGVS (amino-acid)	Matching Registered Transcripts
NP_872622.1:p.Pro40Thr	CA121373 NM_182681.1:c.118C>A