Allele Registry

Canonical Allele Identifier: PA104365

Gene: AMELX HGNC NCBI

ClinVar RCV:

RCV000011892

RCV001588809

ClinVar Variation:

11142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001133.1:p.Pro56Thr	CA121373 NM_001142.2:c.166C>A