Allele Registry

Canonical Allele Identifier: PA109768

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001374700

RCV002307735

ClinVar Variation:

1064674

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val480Asp	CA368841178 NM_000441.2:c.1439T>A