Canonical Allele Identifier: PA2580103960
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195245
ClinVar RCV Id: RCV002628525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Arg752Cys
CA4433532
NM_000111.3:c.2254C>T