Canonical Allele Identifier: PA132676
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val570Ile
CA132675
NM_000441.2:c.1708G>A