Allele Registry

Canonical Allele Identifier: PA109364

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000036444

RCV000169242

RCV000489866

RCV001004645

RCV001375472

ClinVar Variation:

43510

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Gly497Ser	CA261413 NM_000441.2:c.1489G>A