Allele Registry

Canonical Allele Identifier: PA915966109

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001004637

RCV001869296

ClinVar Variation:

691512

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Thr410Lys	CA368839271 NM_000441.2:c.1229C>A