Allele Registry

Canonical Allele Identifier: PA109653

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

19865

ClinVar RCV:

RCV000005096

RCV000005097

RCV000154350

RCV001057908

ClinVar Variation:

4826

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Thr721Met	CA253308 NM_000441.2:c.2162C>T