Canonical Allele Identifier: PA645428230
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 358539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Cys596Gly
CA4433686
NM_000111.3:c.1786T>G