Allele Registry

Canonical Allele Identifier: PA109736

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000036506

RCV000169244

RCV000724118

RCV001004629

RCV001291246

RCV001814026

ClinVar Variation:

43566

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val239Asp	CA261438 NM_000441.2:c.716T>A