Allele Registry

Canonical Allele Identifier: PA109674

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000005107

RCV000036449

RCV001229712

RCV003472970

ClinVar Variation:

4836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Tyr530His	CA253313 NM_000441.2:c.1588T>C