Allele Registry

Canonical Allele Identifier: PA645387338

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000413685

ClinVar Variation:

372827

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ala362Asp	CA16042657 NM_000441.2:c.1085C>A