Allele Registry

Canonical Allele Identifier: PA143850

Gene: SLC26A8 HGNC NCBI

ClinVar Variation Id: 50910

HGVS (amino-acid)	Matching Registered Transcripts
NP_443193.1:p.Glu812Lys	CA143849 NM_052961.4:c.2434G>A