Canonical Allele Identifier: PA132710
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly740Ser
CA132709
NM_000441.2:c.2218G>A