Allele Registry

Canonical Allele Identifier: PA2573170159

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001889500

RCV002553560

ClinVar Variation:

1390239

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Trp482Ser	CA4432825 NM_000441.2:c.1445G>C