Canonical Allele Identifier: PA126860
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16761
ClinVar RCV Id: RCV000018246
ClinVar Variation Id: 810173
ClinVar RCV Id: RCV000998891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Trp462Ter