Allele Registry

Canonical Allele Identifier: PA658826958

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000670687

RCV001855545

ClinVar Variation:

554960

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Thr485Met	CA4432828 NM_000441.2:c.1454C>T