Allele Registry

Canonical Allele Identifier: PA658826937

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

544310

ClinVar RCV:

RCV000674416

ClinVar Variation:

558188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Pro297Gln	CA368835458 NM_000441.2:c.890C>A