Allele Registry

Canonical Allele Identifier: PA915966115

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001004644

ClinVar Variation:

691515

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val483Glu	CA368841199 NM_000441.2:c.1448T>A