Allele Registry

Canonical Allele Identifier: PA109433

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000005100

RCV000036437

RCV000413198

RCV001004641

ClinVar Variation:

4829

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Leu445Trp	CA253309 NM_000441.2:c.1334T>G