Canonical Allele Identifier: PA132676
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43521
ClinVar RCV Id: RCV000036456 RCV000497745 RCV000673671 RCV002496562 RCV003473268 RCV004534763
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Amino-acid Alleles

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