Allele Registry

Canonical Allele Identifier: PA658668684

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000515723

ClinVar Variation:

446461

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Asp669Glu	CA368843815 NM_000441.2:c.2007C>A CA368843816 NM_000441.2:c.2007C>G