Allele Registry

Canonical Allele Identifier: PA102245

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049416

ClinVar Variation:

56007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Ser206Pro	CA144111 NM_000111.3:c.616T>C