Allele Registry

Canonical Allele Identifier: PA259847

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000023571

RCV000055756

RCV000355352

RCV000586327

RCV001004172

RCV001050109

RCV001810418

ClinVar Variation:

65558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Val341del	CA259846 NM_000112.4:c.1020_1022del