Canonical Allele Identifier: PA109612
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4830
ClinVar RCV Id: RCV000005101 RCV000036499 RCV000824763 RCV000770869 RCV001389159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr193Ile
CA253310
NM_000441.2:c.578C>T