Allele Registry

Canonical Allele Identifier: PA109241

Gene: SLC26A4 HGNC NCBI

ClinVar Variation Id: 446453

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Asn392Tyr	CA4432714 NM_000441.2:c.1174A>T