Allele Registry

Canonical Allele Identifier: PA109463

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

679194

ClinVar RCV:

RCV001004625

RCV001389158

RCV003235420

ClinVar Variation:

691508

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Met147Val	CA4432481 NM_000441.2:c.439A>G