Allele Registry

Canonical Allele Identifier: PA658826911

Gene: SLC26A4 HGNC NCBI

ClinVar Variation Id: 552271

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Glu29Gly	CA368845005 NM_000441.2:c.86A>G