Allele Registry

Canonical Allele Identifier: PA109423

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000005086

RCV000036505

RCV000524013

RCV000824766

RCV001089560

RCV001375179

RCV004528073

ClinVar Variation:

4817

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Leu236Pro	CA261437 NM_000441.2:c.707T>C