Canonical Allele Identifier: PA109344
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301849
ClinVar Variation Id: 2776290
ClinVar RCV Id: RCV003663105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly102Arg
CA368845852
NM_000441.2:c.304G>A
CA368845853
NM_000441.2:c.304G>C