Allele Registry

Canonical Allele Identifier: PA102202

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049390

ClinVar Variation:

55981

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Lys521Asn	CA144067 NM_000111.3:c.1563G>C CA368850954 NM_000111.3:c.1563G>T