Allele Registry

Canonical Allele Identifier: PA109373

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000036467

RCV000778812

RCV000801210

RCV001161291

RCV001824586

RCV002291269

ClinVar Variation:

43532

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Gly672Glu	CA261423 NM_000441.2:c.2015G>A