Allele Registry

Canonical Allele Identifier: PA109355

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000005090

RCV000036501

RCV000308471

RCV000344627

RCV000824764

RCV004528077

ClinVar Variation:

4821

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Gly209Val	CA253304 NM_000441.2:c.626G>T