Allele Registry

Canonical Allele Identifier: PA645387567

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000410627

ClinVar Variation:

371298

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val650Asp	CA16041115 NM_000441.2:c.1949T>A