Allele Registry

Canonical Allele Identifier: PA121380

Gene: AMELX HGNC NCBI

ClinVar RCV:

RCV000011896

ClinVar Variation:

11146

HGVS (amino-acid)	Matching Registered Transcripts
NP_872621.1:p.Trp4Ser	CA121379 NM_182680.1:c.11G>C