Allele Registry

Canonical Allele Identifier: PA109453

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

19861

ClinVar RCV:

RCV000005091

ClinVar Variation:

4822

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Lys369Glu	CA253305 NM_000441.2:c.1105A>G