Allele Registry

Canonical Allele Identifier: PA3057517807

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV005200636

ClinVar Variation:

3720766

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ile363Val	CA4432676 NM_000441.2:c.1087A>G