Allele Registry

Canonical Allele Identifier: PA645387546

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000358013

ClinVar Variation:

285774

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Asp618Asn	CA10605240 NM_000441.2:c.1852G>A