Allele Registry

Canonical Allele Identifier: PA102138

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049406

RCV003556125

ClinVar Variation:

55997

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Gly120Ser	CA144093 NM_000111.3:c.358G>A