Allele Registry

Canonical Allele Identifier: PA645387606

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000454307

RCV001004649

RCV002522746

ClinVar Variation:

402277

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Phe683Ser	CA16609565 NM_000441.2:c.2048T>C