Canonical Allele Identifier: PA2580115194
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2268265
ClinVar RCV Id: RCV002825943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly738Ser
CA4433077
NM_000441.2:c.2212G>A