Allele Registry

Canonical Allele Identifier: PA274071

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000169232

RCV000214962

RCV000677335

RCV001850394

RCV002498842

RCV004528923

ClinVar Variation:

188878

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Arg185Thr	CA274070 NM_000441.2:c.554G>C