Allele Registry

Canonical Allele Identifier: PA109573

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001004648

ClinVar Variation:

691517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ser666Phe	CA368843797 NM_000441.2:c.1997C>T