Allele Registry

Canonical Allele Identifier: PA132655

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000036422

RCV000275313

RCV000367654

RCV000906081

RCV004541094

ClinVar Variation:

43491

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ala357Thr	CA132654 NM_000441.2:c.1069G>A