Allele Registry

Canonical Allele Identifier: PA915966127

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

679202

ClinVar RCV:

RCV001004647

ClinVar Variation:

691516

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ser657Asn	CA368843741 NM_000441.2:c.1970G>A