Allele Registry

Canonical Allele Identifier: PA2830415871

Gene: AMELX HGNC NCBI

ClinVar RCV:

RCV000011890

ClinVar Variation:

11140

HGVS (amino-acid)	Matching Registered Transcripts
NP_872622.1:p.Thr21Ile	CA121369 NM_182681.1:c.62C>T